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Crystallization and second harmonic generation in potassium–sodium niobiosilicate glasses

Authors :
Antonio Aronne
Esther Fanelli
Pasquale Pernice
Simone Peli
Gabriele Ferrini
Claudio Giannetti
Aronne, Antonio
Fanelli, Esther
Pernice, Pasquale
S., Peli
C., Giannetti
G., Ferrini
Source :
Journal of Solid State Chemistry. 182:2796-2800
Publication Year :
2009
Publisher :
Elsevier BV, 2009.

Abstract

Transparent glasses having molar composition (23-x)K{sub 2}O.xNa{sub 2}O.27Nb{sub 2}O{sub 5}.50SiO{sub 2} (x=0, 5, 10, 15 and 23) have been synthesized by the melt-quenching technique and their devitrification behaviour has been investigated by DTA and XRD. Depending on the composition, the glasses showed a glass transition temperature in the range 660-680 deg. C and devitrified in several steps. XRD measurements showed that the replacement of K{sub 2}O by Na{sub 2}O strongly affects the crystallization behaviour. Particularly, in the glasses with only potassium or low sodium content the first devitrification step is related to the crystallization of an unidentified phase, while in the glass containing only sodium, NaNbO{sub 3} crystallizes. For an intermediate sodium content (x=10 and 15) a potassium sodium niobate crystalline phase, belonging to the tungsten-bronze family, is formed by bulk nucleation. This system looks promising to produce active nanostructured glasses as the tungsten-bronze type crystals have ferroelectric, electro-optical and non-linear optical properties. Preliminary measurements evidenced SHG activity in the crystallized glasses containing this phase. - Graphical abstract: Synthesis of glasses (23-x)K{sub 2}O.xNa{sub 2}O.27Nb{sub 2}O{sub 5}.50SiO{sub 2} (x=0, 5, 10, 15 and 23) from which SHG active phases crystallize by bulk nucleation for non-linear optical nanostructured glasses.

Details

ISSN :
00224596
Volume :
182
Database :
OpenAIRE
Journal :
Journal of Solid State Chemistry
Accession number :
edsair.doi.dedup.....a5bf496816a46a20be69e9464dc2605a
Full Text :
https://doi.org/10.1016/j.jssc.2009.07.052